Reconstitution system to administer a drug via a high vacuum vial with integrated vent conduit

ABSTRACT

A reconstitution device includes a body, a first piercing member located at a first end of the body, and a receptacle located at the second end of the body. The receptacle includes a collar configured to engage a vial, and a cap extending from the collar and holding a second piercing member. The second piercing member is disposed within the collar. The reconstitution device includes a first fluid pathway formed within and extending from the first piercing member to the second piercing member. The reconstitution device includes a second fluid pathway formed within and extending from the second piercing member to a portion of the body between the first piercing member and the second piercing member.

BACKGROUND

Medical therapy often requires the intravenous administration of fluidsto correct electrolyte imbalance, medicated solutions, and/or nutrientsto provide nutrition to patients unable to receive oral or enteralnutrition. Intravenous (“IV”) fluids are generally available in asepticsingle- or multi-chamber flexible containers that include anadministration port and a medication port. An IV administration set istypically inserted into a flexible container, such as a multi-chamber IVbag, via the administration port to allow administration of the fluidsfrom the flexible container to the patient. Likewise, medications and/ornutrients can be injected, into the flexible container, via themedication port.

Certain active agents, such as medications and nutrients, which may beunstable in liquid form, are stored in dry form. For example, activeagents may be unstable at the pH of the IV fluid, susceptible to damagevia light, or have other instability, thus requiring dry form storage.Dry form active agents may be stored in glass vials, sealed with rubberstoppers, or be stored in other containers such as plastic containers,ampoules, or in small bags that may be closed with standard screw caps.Prior to being administered to a patient, the dry form active agents arereconstituted. Reconstitution typically includes the removal of aprotective cover to expose the rubber stopper, wiping the stopper withan antiseptic wipe, adding a diluent to the vial by inserting a needleof a syringe through the rubber stopper and depositing the contents ofthe syringe, such as the diluent, into the vial, and shaking the vial tofully dissolve or suspend the active agents. Subsequently, the resultingreconstituted solution or suspension is withdrawn from the vial byinserting a needle of a syringe through the rubber stopper, aspiratingthe solution or suspension into the syringe, and injecting the contentsof the syringe into the flexible container via the medication port.

The above procedure is cumbersome and prone to spillage. An improvedsystem and method for using a reconstitution device to administermedications via IV bags, is needed accordingly.

SUMMARY

To improve the administration of medications via IV bags, a patientmedication delivery paradigm is provided herein. To implement animproved way of medication administration, a reconstitution device,system, and method is disclosed. More specifically, a reconstitutiondevice is provided to establish a fluid pathway between a source (e.g.,a drug vial) and a location (e.g., an intravenous (“IV”) bag), whichincludes a vent conduit to improve reconstitution, especially withrespect to multi-chamber bags.

In light of the disclosure herein, and without limiting the scope of theinvention in any way, in a first aspect of the present disclosure, whichmay be combined with any other aspect listed herein unless specifiedotherwise, a reconstitution device includes a body, a first piercingmember located at a first end of the body, and a receptacle located atthe second end of the body. The receptacle includes a collar configuredto engage a vial, and a cap extending from the collar and holding asecond piercing member. The second piercing member is disposed withinthe collar. The reconstitution device includes a first fluid pathwayformed within and extending from the first piercing member to the secondpiercing member. The reconstitution device includes a second fluidpathway formed within and extending from the second piercing member to aportion of the body between the first piercing member and the secondpiercing member.

In a second aspect of the present disclosure, which may be combined withany other aspect listed herein unless specified otherwise, the cap isformed integrally with the collar.

In a third aspect of the present disclosure, which may be combined withany other aspect listed herein unless specified otherwise, the collar iscylindrical and is configured to concentrically engage the vial.

In a fourth aspect of the present disclosure, which may be combined withany other aspect listed herein unless specified otherwise, the collarengages the vial, such that the second piercing member extends into thevial, and such that the second piercing member is placed in fluidcommunication with the vial.

In a fifth aspect of the present disclosure, which may be combined withany other aspect listed herein unless specified otherwise, the firstpiercing member is configured to pierce an intravenous (“IV”) bag port,such that the first piercing member is placed in fluid communicationwith the IV bag port.

In a sixth aspect of the present disclosure, which may be combined withany other aspect listed herein unless specified otherwise, the secondfluid pathway forms a vent conduit.

In a seventh aspect of the present disclosure, which may be combinedwith any other aspect listed herein unless specified otherwise, aremovable plug is fitted within the second fluid pathway at the portionof the body between the first piercing member and the second piercingmember.

In a eighth aspect of the present disclosure, which may be combined withany other aspect listed herein unless specified otherwise, the removableplug forms a hermetic seal with the portion of the body between thefirst piercing member and the second piercing member.

In a ninth aspect of the present disclosure, which may be combined withany other aspect listed herein unless specified otherwise, the vial isinitially sealed under a vacuum.

In a tenth aspect of the present disclosure, which may be combined withany other aspect listed herein unless specified otherwise, areconstitution system includes a drug vial, a fluid container, and areconstitution device. The reconstitution device includes a body, afirst piercing member located at a first end of the body, and areceptacle located at a second end of the body. The receptacle includesa collar configured to engage the drug vial, and a cap extending fromthe collar and holding a second piercing member. The second piercingmember is disposed within the collar. The reconstitution device includesa first fluid pathway formed within and extending from the firstpiercing member to the second piercing member. The reconstitution deviceincludes a second fluid pathway formed within and extending from thesecond piercing member to a portion of the body between the firstpiercing member and the second piercing member.

In a eleventh aspect of the present disclosure, which may be combinedwith any other aspect listed herein unless specified otherwise, thefirst piercing member extends into the fluid container, and the collarengages the drug vial such that the second piercing member extends intothe drug vial, and such that the fluid container is placed in fluidcommunication with the drug vial via the first fluid pathway.

In a twelfth aspect of the present disclosure, which may be combinedwith any other aspect listed herein unless specified otherwise, thereconstitution system further includes a plug disposed along the portionof the body between the first piercing member and the second piercingmember.

In a thirteenth aspect of the present disclosure, which may be combinedwith any other aspect listed herein unless specified otherwise, the plugis removable and, responsive to the plug being removed, the drug vial isplaced in fluid communication with an external environment via thesecond fluid pathway.

In a fourteenth aspect of the present disclosure, which may be combinedwith any other aspect listed herein unless specified otherwise, air fromthe external environment (i) flows into the drug vial via the secondfluid pathway, and (ii) pushes a reconstituted solution from the drugvial into the fluid container via the first fluid pathway.

In a fifteenth aspect of the present disclosure, which may be combinedwith any other aspect listed herein unless specified otherwise, the drugvial contains one of a pharmaceutical agent or a nutritional supplement.

In a sixteenth aspect of the present disclosure, which may be combinedwith any other aspect listed herein unless specified otherwise, the drugvial is initially sealed under a vacuum.

In a seventeenth aspect of the present disclosure, which may be combinedwith any other aspect listed herein unless specified otherwise, the drugvial is formed of an ultraviolet (“UV”) light blocking material.

In a eighteenth aspect of the present disclosure, which may be combinedwith any other aspect listed herein unless specified otherwise, thereconstitution system further includes an intravenous (“IV”) linepositioned and arranged to deliver a fluid from the fluid container to apatient.

In a nineteenth aspect of the present disclosure, which may be combinedwith any other aspect listed herein unless specified otherwise, thereconstitution system further includes an infusion pump in operablecommunication with the IV line.

In a twentieth aspect of the present disclosure, which may be combinedwith any other aspect listed herein unless specified otherwise, a drugreconstitution method includes enabling engagement of a first piercingmember with a fluid container and enabling engagement of a secondpiercing member with a drug vial, such that intravenous (“IV”) fluid mayflow along a first fluid pathway formed within and extending from thefluid container to the drug vial. The method includes enabling mixing ofthe IV fluid with an agent located within the drug vial to form a mixeddrug. The method includes enabling removal of a plug, such that air froman external environment may flow along a second fluid pathway formedwithin and extending from the external environment to the drug vial. Airpressure in the external environment causes air to (i) flow into thedrug vial via the second fluid pathway, and (ii) push the mixed drugfrom the drug vial to the fluid container via the first fluid pathway.

In a twenty first aspect of the present disclosure, any of thestructure, functionality, and alternatives discussed in connection withany of FIGS. 1 to 7 may be combined with any of the structure,functionality, and alternatives discussed in connection with any otherone or more of FIGS. 1 to 7.

In light of the disclosure and aspects set forth herein, it isaccordingly an advantage of the present disclosure to provide areconstitution system that ensures complete reconstitution andsubsequent infusion of a drug from a drug vial directly into a flexiblecontainer.

It is another advantage of the present disclosure to provide areconstitution system that reduces drug degradation by reconstitutingthe drug and immediately delivering it to the flexible container. Theparticular system may be further configured to limit environmentaldegradation by avoiding solution-interaction with outside factors, suchas light or air.

It is a further advantage of the present disclosure to provide areconstitution system that ensures the contents of the vial, such as thereconstituted drug, are diluted prior to being administrated to thepatient to prevent any medical or efficacy risks based on osmolarity.

It is yet another advantage of the present disclosure to provide aready-to-use reconstitution system configured to accept vials directly.

It is yet a further advantage of the present disclosure to provide areconstitution system avoiding tedious preparation steps involved withtypical dried drug reconstitution by accepting vials directly.

It is still another advantage of the present disclosure to pre-plug thevial to ensure that drug prescriptions and deliveries are notinadvertently missed by medical professionals.

In yet another advantage of the present disclosure, each discretecomponent of the reconstitution system may be processed, sterilized, andhandled separately on a component-by-component basis.

In yet a further advantage of the present disclosure, the reconstitutiondevice may be particularly applicable for use with multi-chamber IVbags.

Moreover, an advantage of the present disclosure is to provide areconstitution system ensuring that microbiological contamination riskis minimized by accepting pre-plugged vials in a sterile manner.

Additional features and advantages of the disclosed devices, systems,and methods are described in, and will be apparent from, the followingDetailed Description and the Figures. The features and advantagesdescribed herein are not all-inclusive and, in particular, manyadditional features and advantages will be apparent to one of ordinaryskill in the art in view of the figures and description. Also, anyparticular embodiment does not have to have all of the advantages listedherein. Moreover, it should be noted that the language used in thespecification has been selected for readability and instructionalpurposes, and not to limit the scope of the inventive subject matter.

BRIEF DESCRIPTION OF THE FIGURES

Understanding that figures depict only typical embodiments of theinvention and are not to be considered to be limiting the scope of thepresent disclosure, the present disclosure is described and explainedwith additional specificity and detail through the use of theaccompanying figures. The figures are listed below.

FIG. 1 is a top plan view of a reconstitution device, drug vial, andmulti-chamber bag, according to an example embodiment of the presentdisclosure.

FIG. 2 is a sectioned elevation view of a reconstitution device, drugvial, and multi-chamber bag, according to an example embodiment of thepresent disclosure.

FIG. 3 is a sectioned elevation view of a reconstitution device and drugvial engaging with a multi-chamber bag, according to an exampleembodiment of the present disclosure.

FIG. 4 is a rotated sectioned elevation view of the reconstitutiondevice and drug vial engaging with a multi-chamber bag of FIG. 1,according to an example embodiment of the present disclosure.

FIG. 5 is a sectioned elevation view of a reconstitution device and drugvial engaging with a multi-chamber bag during plug removal, according toan example embodiment of the present disclosure.

FIG. 6 is a sectioned elevation view of a reconstitution device and drugvial engaging with a multi-chamber bag during plug reattachment,according to an example embodiment of the present disclosure.

FIG. 7 is a schematic view of one embodiment of a system employing anyof the reconstitution devices described herein.

DETAILED DESCRIPTION

Certain embodiments described herein relate generally to the field ofintravenous (“IV”) administration of an active agent. More particularly,some embodiments described herein relate to the reconstitution of anactive agent in a vial, delivery to a flexible container, and subsequentIV administration of the active agent using the flexible container andan IV administration set.

As discussed herein, adding a dried drug to an IV bag typically includesseveral tedious steps. For example, a medical professional may berequired to remove a protective cover from a vial, wipe a stopper of thevial, add diluent to the vial, and shake the vial. The drug then has tobe withdrawn from the vial and injected into, for example, an IV bag.

Typical commercially available vial reconstitution systems (e.g., theBaxter Vial-Mate™ system) are configured such that the drug contained inthe vial is added into a single chamber IV bag directly, via a port. Insuch systems, the drug from the vial is mixed with fluid within theentire single chamber IV bag, such as saline, prior to beingadministered to the patient. For example, the drug is delivered into thesingle chamber IV bag, via a medication port, mixes with the fluid ofthe single chamber IV bag, and is then administered to the patient viaan administration port (e.g., by an IV set connected to the singlechamber IV bag at the administration port). In this delivery paradigm,once the vial is connected to the IV bag, pressure is applied onto theIV bag to “push” liquid from the IV bag into the vial, forreconstituting the drug. The system is then flipped upside down, andpressure is applied to the bag to “push” headspace gas from the IV baginto the vial. The headspace gas consequently forces the reconstituteddrug back into the IV bag.

The above delivery paradigm is particularly problematic withmulti-chamber IV bags, which typically have frangible seals that openwhen pressure is applied to the bag. Further, multi-chamber IV bags aretypically underfilled, thus making it difficult if not impossible toapply pressure to “push” headspace gas into the vial.

The reconstitution devices, systems, and methods disclosed herein areconfigured so that the vial containing the drug is connected directlywith the multi-chamber IV bag. The connection allows for both an initialreconstitution in the vial, permitting fluid to flow from themulti-chamber IV bag to the vial, and a secondary reconstitution as thereconstituted drug travels directly into the multi-chamber IV bag fromthe vial. Implementation of an integrated vent conduit ensures thatreconstituted solution can travel back into the IV bag, withoutrequiring the application of pressure at the IV bag for “pushing”headspace gases. Thus, the devices, systems, and methods disclosedherein are particularly applicable in circumstances concerningunderfilled bags, such as multi-chamber IV bags. The presentconfiguration enhances the efficacy by which a drug is reconstituted inthe vial and delivered subsequently to a patient. Further, the vial mayinitially be sealed and placed under a vacuum, thus eliminating the needto “push” liquid from the IV bag into the vial. When initiallyreconstituted, the vacuum may further enhance the efficacy by which adrug is reconstituted in a vial.

Referring now to the drawings and in particular to FIG. 1, oneembodiment of the reconstitution device and multi-chamber bag of thepresent disclosure is illustrated. Multi-chamber bag 10 includes severaldiscrete chambers separated by frangible barriers, including firstchamber 12, second chamber 14, third chamber 16, and fourth chamber 18.It should be appreciated that multi-chamber bag 10 could include more,or less, than four chambers. In an embodiment, first chamber 12 holdslipids in liquid form, second chamber 14 holds amino acids in liquidform, third chamber 16 holds trace elements in liquid form, and fourthchamber 18 holds glucose in liquid form. Each of the chambers 12, 14,16, 18 includes a respective administration port 20, 22, 24, 26.Multi-chamber bag 10 may be constructed of any suitable plastic orrubber material, such as polyvinyl chloride (“PVC”), non-DEHP PVC,Krayton polypropylene mixture, or other similar materials.

As illustrated, reconstitution device 28 engages with administrationport 20 (associated with first chamber 12). It should be appreciatedthat reconstitution device 28 could engage with any of theadministration ports and/or chambers mentioned above. Reconstitutiondevice 28 also engages with a vial 30, discussed in greater detailherein. Any of the device engagements discussed herein may be via a luerconnector, tube connector, snap fit, interference fit, or any otherrelated means for connection. Via the vial engagement, a dried drug fromvial 30 is reconstituted with fluid from the first chamber 12, oralternatively several chambers if their seals have been broken, and thereconstituted drug is subsequently delivered into multi-chamber bag 10,for further reconstitution with the entire multi-chamber bag 10 andfuture delivery to a patient. For example, multi-chamber bag 10 mayfurther include a port or connection for engagement with an IV deliverytube, connected to a patient. Multi-chamber bag 10 may further include aloop 32, for hanging the bag on a stand, as discussed in greater detailherein.

FIG. 2 is a sectioned view of the reconstitution device 28 andmulti-chamber bag 10 of FIG. 1, according to an example embodiment ofthe present disclosure. As illustrated, multi-chamber bag 10 initiallyincludes a membrane 34 at administration port 20.

Reconstitution device 28 includes a piercing end 36, a body 38, and aretaining end 40. Reconstitution device 28 may be constructed of anysuitable plastic or rubber material, such as polyvinyl chloride (“PVC”),non-DEHP PVC, Krayton polypropylene mixture, or other similar materials.

Retaining end 40 is configured to engage vial 30 (e.g., via concentricengagement). Vial 30 may be fitted with a stopper 42, which may be arubber stopper, a plastic stopper, and/or include a foil cover, or beany other similar structure for sealing vial 30. Stopper 42 may protectthe contents of vial 30 from environmental factors, such as ambient air.In an embodiment, the contents of vial 30 include a dried drug 44. In anembodiment, vial 30 is formed of an ultraviolet (“UV”) light blockingmaterial, which may further protect the contents of vial 30 fromenvironmental factors, such as light.

Specifically, regarding the concentric engagement of device 28 to vial30, retaining end 40 of reconstitution device 28 includes a cap 46.Retaining end 40 further includes a cylindrical collar 48. Cap 46 may beformed integrally with collar 48, or be attached to retaining end 40. Inalternative embodiments, collar 48 may have differently shapedcross-sections (e.g., hexagonal, square, triangular, or other suitablegeometric shape). Cylindrical collar 48 is configured to engage vial 30(e.g., via concentric engagement).

In the illustrated embodiment, the stopper-side of vial 30 may bereceived within cylindrical collar 48 of device 28, such that thecylindrical collar 48 is disposed around the outside of the stopper-sideof vial 30. Vial 30 typically contains an active agent such as apharmaceutical agent or a nutritional supplement. The active agent maybe present as a dried drug 44, such as a powder obtained bylyophilization. Alternatively, the active agent is present in an aqueoussolution or suspension, or other typical liquid form. The inner surfaceof collar 48 may include a plurality of ridges 50 that are configured toengage, e.g., via a spring-like deformation, to press-fit or snap-fitover the stopper-side of vial 30, such that the stopper-side of vial 30is retained inside the plurality of ridges 50 of the collar 48.

Reconstitution device 28 further includes a first piercing member 52 anda second piercing member 54. First piercing member 52 and secondpiercing member 54 may be made of metal (e.g., stainless steel), medicalgrade plastic, or other suitable material. A first fluid pathway 56extends between first piercing member 52 and second piercing member 54.Specifically, cap 46 extends from collar 48 and holds second piercingmember 54. Second piercing member 54 is disposed within collar 48. Asconfigured, first piercing member 52 is configured to engage withadministration port 20 of multi-chamber bag 10; likewise, secondpiercing member 54 is configured to engage with vial 30. In anembodiment, at least one of the first piercing member 52 or the secondpiercing member 54 may include or form a syringe needle or a plasticspike.

Reconstitution device 28 further includes a plug 58, disposed along aportion of body 38 between piercing end 36 and retaining end 40.Specifically, plug 58 may be removably attached to a receptacle 60 alongbody 38. Generally, plug 58 is configured to form a hermetic seal withreceptacle 60 when engaged. In various embodiments, plug 58 engages withreceptacle 60 via a threaded fit, snap fit, or other suitable fit. In anembodiment, plug 58 further includes an o-ring or other gasket. A secondfluid pathway 62 extends between receptacle 60 and second piercingmember 54.

FIG. 3 is a section view of the reconstitution device 28 of FIG. 1,further illustrating the engagement with multi-chamber bag 10, accordingto an example embodiment of the present disclosure. As previouslyillustrated with respect to FIG. 2, FIG. 3 also shows administrationport 20 of multi-chamber bag 10 includes membrane 34 (e.g., a removablemembrane or a pierceable membrane). Membrane 34 may initially preventpremature flow from multi-chamber bag 10. Membrane 34 may further ensurethat a vacuum exists within the various fluid pathways communicatingwith vial 30 during reconstitution, to advantageously generatepressurized fluid streams for reconstitution, as described in greaterdetail below. Membrane 34 may also reduce or eliminate leakage frommulti-chamber bag 10.

First piercing member 52 is, in the illustrated embodiment, configuredto pierce an administration port (e.g., an IV bag port) at membrane 34,so that the first piercing member 52 is in fluid communication withadministration port 20 and thus with multi-chamber bag 10.Administration port 20 may be connected to multi-chamber bag 10 or maybe formed integrally with multi-chamber bag 10.

As illustrated in FIG. 3, vial 30 is engaged within collar 48 such thatsecond piercing member 54 pierces stopper 42 of vial 30. In oneembodiment, the user pushes vial 30 onto cap 46 to secure engagementbetween the vial 30 and the collar 48. In one embodiment, secondpiercing member 54 pierces through the stopper 42 (e.g., a rubberstopper) of vial 30 and extends into vial 30. In a related embodiment,engagement between the collar 48 and the vial 30 may further includerotation or twisting of the vial 30. For example, the collar 48 mayinclude inner threads, and the vial 30 may include outer threads, suchthat a threaded engagement between the vial 30 and the collar 48 isimplemented for secure engagement between the components.

Once engaged, multi-chamber bag 10 is in fluid communication with thevial 30 via first fluid pathway 56 that extends from first piercingmember 52 to second piercing member 54. In an embodiment, vial 30 isinitially sealed and under a vacuum, prior to engagement with collar 48(e.g., a low pressure such as 100 mbar, which is less than ambient airpressure).

It should be appreciated that the piercing described above for firstpiercing member 52 and second piercing member 54 happens nearlysimultaneously in one embodiment. For example, once first piercingmember 52 pierces the administration port 20 (e.g., an IV bag port) atmembrane 34, first piercing member 52 is in fluid communication withadministration port 20; thus, liquid may flow from administration port20 into the reconstitution device 28 via the first fluid pathway 56. Toensure that liquid does not inadvertently spill out of the secondpiercing member 54 (e.g., via first fluid pathway 56), the secondpiercing member 54 pierces stopper 42 of vial 30 immediately after thefirst piercing member 52 pierces the administration port 20 (e.g.,nearly simultaneously). In this way, inadvertent spilling is prevented.

After the piercing of members 52 and 54, fluid in multi-chamber bag 10may flow directly from the first piercing member 52 to the secondpiercing member 54 via the first fluid pathway 56, and consequently intovial 30. Flow into vial 30 via first fluid pathway 56 can becharacterized as a pressurized fluid stream (e.g., jet stream). Becausevial 30 was initially sealed and under a vacuum prior to engagement withcollar 48, engagement causes fluid from multi-chamber bag 10 to berapidly drawn into vial 30 by the negative pressure. The initial draw offluid may generate a pressurized fluid stream from the second piercingmember 54 (e.g., a jet stream) into vial 30. In certain embodiments, apressurized fluid stream is advantageous for mixing and reconstituting adried drug within vial 30. The magnitude of the vacuum in vial 30 may beadjusted, to obtain an optimal mixing effect and/or to obtain thedesired filling volume. The vacuum also aids in reducing or eliminatingproblems in removing air compared to vial 30 instead being underatmospheric pressure. As fluid from multi-chamber bag 10 flows into vial30, dried drug 44 is reconstituted. Dried drug 44 illustrated in FIG. 2is no longer shown in FIG. 3 because the drug has been reconstitutedwith fluid from multi-chamber bag 10.

The reconstituted drug within vial 30 next needs to be sent back intomulti-chamber bag 10. Reconstitution device 28 is capable of performingthis operation via second fluid pathway 62, also referred to herein as avent or vented conduit. The process of flowing the reconstituted drugback into bag 10 is performed in connection with FIGS. 4 to 6, whichillustrate engagement of reconstitution device 28 to multi-chamber bag10, according to example embodiments of the present disclosure.

As illustrated in FIG. 4, reconstitution device 28 and related vial 30are rotated vertically to an upside-down configuration. Plug 58 is thenremoved from receptacle 60, as illustrated by FIG. 5. Alternatively,instead of physically removing plug 58, the user merely moves plug 58from a closed state to an opened state. By removing plug 58 fromreceptacle 60 (or opening plug 58), vial 30 is placed in fluidcommunication with an external environment, such as a medicalpreparation room, via second fluid pathway 62. In an embodiment,reconstitution device 28 further includes an air filter, such as a 0.22μm air filter, disposed along receptacle 60 between plug 58 and secondfluid pathway 62. In a different embodiment, the air filter is disposedalong second fluid pathway 62.

As previously noted, vial 30 is initially sealed and under a vacuum.Likewise, the contents of multi-chamber bag 10 are sealed at a lowerpressure. Thus, the entire system, prior to removal of plug 58, is at asub-atmospheric pressure. For this reason, removal of plug 58 causesatmospheric air from the external environment to flow into vial 30 viasecond fluid pathway 62, and subsequently push the reconstitutedmaterial from the vial 30 to multi-chamber bag 10 via first fluidpathway 56. Once reconstituted material flows into multi-chamber bag 10,plug 58 is then re-attached to receptacle 60 (or closed), as illustratedby FIG. 6.

In an alternate embodiment, reconstitution device 28 may additionally oralternatively include a valve to replace plug 58. For example, auser-operated valve may be implemented, such that the user mayselectively open and close receptacle 60 via the valve, therebycontrolling when second fluid pathway 62 communicates with the externalenvironment. In a related embodiment, user-operated valve may furtherprovide the user with the ability to selectively open and close firstfluid pathway 56. It should be appreciated that the user-operated valvemay be positioned at any location along reconstitution device 28 and/orthere could be multiple valves (e.g., one valve for each of first fluidpathway 56 and second fluid pathway 62). In various embodiments, theuser-operated valve may be a ball valve, a gate valve, a globe valve, acheck valve, or other related valves.

In an alternate embodiment, reconstitution device 28 may be implementedwith an IV bag that is initially empty and under a vacuum or partialvacuum. For example, the reconstitution device 28 with vial 30 isconnected to an empty IV bag (e.g., via administration port 20). Theempty IV bag may then be subsequently filled with any desired solution,such as saline or glucose, through a dedicated port. This may beadvantageous for applications where providing the solution ahead of timeis costly or difficult. In this alternative embodiment, the solution forthe IV bag may be prepared and the IV bag may be filled duringadministration. As solution is added to the empty IV bag (that isalready connected to reconstitution device 28), reconstitution may occuras described above.

FIG. 7 illustrates one embodiment of a system 200 employingreconstitution device 28, which is configured to engage with drug vial30 as described above. System 200 includes an IV bag 202 (e.g.,multi-chamber bag 10) hanging from a stand 204 (e.g., via loop 32). TheIV bag 202 may include a fluid, such as saline, glucose, or othersimilar fluid, for delivery to a patient 206. As illustrated, IV bag 202is positioned on the stand 204 to ensure that the IV bag 202 is locatedvertically above the patient 206, which ensures that fluid in the IV bag202 gravity flows to patient 206. Furthermore, the IV bag 202 isillustrated as a single-chamber in FIG. 7; it should be appreciated,however, that IV bag 202 is alternatively a multi-chamber bag (e.g.,multi-chamber bag 10 illustrated in FIG. 1), and that the seals betweenchambers have already been opened in FIG. 7.

System 200 as illustrated includes reconstitution device 28 and vial 30.Reconstitution device 28 is connected to IV bag 202 as previouslydescribed using first piercing member 52, while vial 30 is connected aspreviously described using second piercing member 54. A delivery tube208, such as an IV tube, engages with IV bag 202. Delivery tube 208 isalso connected to patient 206 at an IV location 210. For example,delivery tube 208 may extend to an intra-venous needle inserted into thepatient 206 at the IV location 210.

Delivery tube 208 is configured to convey the fluid in the IV bag 202,mixed with drug 44 from vial 30 in IV bag 202, to the patient 206 at IVlocation 210. While fluid conveyance may be facilitated via gravity dueto IV bag 202 being elevated on the stand 204, additional or alternativemodes of fluid conveyance may be implemented. For example, system 200may use an infusion pump 212, which may for example be a Sigma™ LargeVolume Pump (“LVP”) provided by the assignee of the present disclosure.Infusion pump 212 may control fluid conveyance along delivery tube 208(e.g., from the IV bag 202 to the patient 206 at the IV location 210).In such a case, bag 202 may be located even or vertically below patient206.

With reference to FIGS. 3 and 7, the fluid in the IV bag 202 may travelinto the first piercing member 52 and subsequently travel into the vial30, via the first fluid pathway 56. The fluid mixes with drug 44 in vial30 to form a reconstituted solution. Upon flipping of reconstitutiondevice 28 and vial 30, as illustrated by FIG. 4, and subsequent removal(or opening) of plug 58, as illustrated by FIG. 5, the reconstitutedsolution may then flow from vial 30 to IV bag 202 via first fluidpathway 56. Consequently, as illustrated in FIG. 7, IV fluid from IV bag202 mixed with reconstituted solution may both be delivered, from the IVbag 202, into delivery tube 208. IV fluid from the IV bag 202 and thereconstituted drug solution may then flow to patient 206 via IV location210. In various embodiments, flow to the IV location 210 is conveyed viagravity and/or via infusion pump 212.

The fluid conveyance process described above may, in certainembodiments, include additional steps. For example, the reconstitutiondevice 28 may engage drug vial 30 at the cylindrical collar 48; however,prior to this engagement, the delivery tube 208 may be clamped via atypical medical line clamp. The medical professional may do this toinitially ensure that any inline air (e.g., in delivery tube 208 or inreconstitution device 28) is removed from the system 200, such as bytapping the reconstitution device 28 and/or tube 208.

The above described reconstitution device, system, and method may beused, for example, during a parenteral nutrition therapy. Here,reconstitution may be used to enhance the administration of amultivitamin product that would otherwise be added to a total parenteralnutrition (“TPN”) bag through the medication port. Examples of knownparenteral nutrition products, which could be used with the presentdevice, system, and method, include Olimel®, Oliclinomel, Clinomel,Clinimix®, Numeta®, ClinOleic®, SmofKabiven®, Kabiven®, PeriKabiven®,StructoKabiven, Aminomix, Nutriflex, Nutriflex Lipid, Pediaven products,and the like. In various examples, the reconstitution device 28 may bepermanently connected to a TPN or multi-chamber bag 10, or may be addedto the TPN or multi-chamber bag 10 prior to use.

As used in this specification, including the claims, the term “and/or”is a conjunction that is either inclusive or exclusive. Accordingly, theterm “and/or” either signifies the presence of two or more things in agroup or signifies that one selection may be made from a group ofalternatives.

Without further elaboration, it is believed that one skilled in the artcan use the preceding description to utilize the claimed inventions totheir fullest extent. The examples and embodiments disclosed herein areto be construed as merely illustrative and not a limitation of the scopeof the present disclosure in any way. It will be apparent to thosehaving skill in the art that changes may be made to the details of theabove-described embodiments without departing from the underlyingprinciples discussed. In other words, various modifications andimprovements of the embodiments specifically disclosed in thedescription above are within the scope of the appended claims. Forexample, any suitable combination of features of the various embodimentsdescribed is contemplated. Note that elements recited inmeans-plus-function format are intended to be construed in accordancewith 35 U.S.C. § 112 ¶6. The scope of the invention is therefore definedby the following claims.

The invention is claimed as follows:
 1. A reconstitution devicecomprising: a body; a first piercing member located at a first end ofthe body; a receptacle located at a second end of the body, thereceptacle including a collar configured to engage a vial, and a capextending from the collar and holding a second piercing member, whereinthe second piercing member is disposed within the collar; a first fluidpathway formed within and extending from the first piercing member tothe second piercing member; a second fluid pathway formed within andextending from the second piercing member to a portion of the bodybetween the first piercing member and the second piercing member; and aremovable plug fitted within the second fluid pathway at the portion ofthe body between the first piercing member and the second piercingmember, wherein the removable fitted plug enables the reconstitutiondevice and the vial to be maintained at a sub-atmospheric pressure, andwherein removal of the plug from the second fluid pathway allowsatmospheric air to flow into the vial via the second fluid pathway, theincoming atmospheric air allowing drainage of the reconstituted materialfrom the vial through the first piercing member of the first fluidpathway.
 2. The reconstitution device of claim 1, wherein the cap isformed integrally with the collar.
 3. The reconstitution device of claim1, wherein the collar is cylindrical and is configured to concentricallyengage the vial.
 4. The reconstitution device of claim 1, wherein thecollar engages the vial, such that the second piercing member extendsinto the vial, and such that the second piercing member is placed influid communication with the vial.
 5. The reconstitution device of claim1, wherein the first piercing member is configured to pierce anintravenous (“IV”) bag port, such that the first piercing member isplaced in fluid communication with the IV bag port.
 6. Thereconstitution device of claim 1, wherein the second fluid pathway formsa vent conduit.
 7. The reconstitution device of claim 1, wherein theremovable plug forms a hermetic seal with the portion of the bodybetween the first piercing member and the second piercing member.
 8. Thereconstitution device of claim 1, wherein the vial is initially sealedunder a vacuum.
 9. The reconstitution device of claim 1, wherein thereconstitution device includes a container in fluid communication withthe first fluid pathway, wherein the incoming atmospheric air allows tothe reconstituted material to flow from the vial into the container viathe first piercing member of the first fluid pathway.
 10. Areconstitution system comprising: a drug vial; a fluid container; and areconstitution device, the reconstitution device including a body; afirst piercing member located at a first end of the body; a receptaclelocated at a second end of the body, the receptacle including a collarconfigured to engage the drug vial, and a cap extending from the collarand holding a second piercing member, wherein the second piercing memberis disposed within the collar; a first fluid pathway formed within andextending from the first piercing member to the second piercing member;a second fluid pathway formed within and extending from the secondpiercing member to a portion of the body between the first piercingmember and the second piercing member; and a removable plug fittedwithin the second fluid pathway at the portion of the body between thefirst piercing member and the second piercing member, wherein theremovable fitted plug enables the reconstitution device and the vial tobe maintained at a sub-atmospheric pressure, and wherein removal of theplug from the second fluid pathway allows atmospheric air to flow intothe vial via the second fluid pathway, the incoming atmospheric airallowing drainage of a reconstituted material from the vial through thefirst piercing member of the first fluid pathway, and into thecontainer.
 11. The reconstitution system of claim 10, wherein the firstpiercing member extends into the fluid container, and wherein the collarengages the drug vial such that the second piercing member extends intothe drug vial, and such that the fluid container is placed in fluidcommunication with the drug vial via the first fluid pathway.
 12. Thereconstitution system of claim 10, wherein the plug is removable, andwherein, responsive to the plug being removed, the drug vial is placedin fluid communication with an external environment via the second fluidpathway.
 13. The reconstitution system of claim 12, wherein air from theexternal environment (i) flows into the drug vial via the second fluidpathway, and (ii) pushes a reconstituted solution from the drug vialinto the fluid container via the first fluid pathway.
 14. Thereconstitution system of claim 10, wherein the drug vial contains eithera pharmaceutical agent or a nutritional supplement.
 15. Thereconstitution system of claim 10, wherein the drug vial is initiallysealed under a vacuum.
 16. The reconstitution system of claim 10,wherein the drug vial is formed of an ultraviolet (“UV”) light blockingmaterial.
 17. The reconstitution system of claim 10, wherein thereconstitution device includes an intravenous (“IV”) line positioned andarranged to deliver a fluid from the fluid container to a patient. 18.The reconstitution system of claim 17, wherein the reconstitution deviceincludes an infusion pump in operable communication with the IV line.